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CANNON II PLUS CHRONIC HEMODIALYSIS CATHETER, EDGE CHRONIC HEMODIALYSIS CATHETER, NEXTSTEP(R) RETROGRADE CHRONIC...

Page Type
Cleared 510(K)
510(k) Number
K111117
510(k) Type
Special
Applicant
Teleflex Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
6/30/2011
Days to Decision
70 days
Submission Type
Summary

CANNON II PLUS CHRONIC HEMODIALYSIS CATHETER, EDGE CHRONIC HEMODIALYSIS CATHETER, NEXTSTEP(R) RETROGRADE CHRONIC...

Page Type
Cleared 510(K)
510(k) Number
K111117
510(k) Type
Special
Applicant
Teleflex Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
6/30/2011
Days to Decision
70 days
Submission Type
Summary